A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17439019



Internal ID22496889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:97319633..97319751hg38UCSC Ensembl
chr6:97767509..97767627hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5889483
Supporting Variants
Samples
Known GenesMIR548H3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17439019
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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